Department of Physiology, Anatomy and Genetics, University of Oxford, United Kingdom.
Curr Gene Ther. 2012 Aug;12(4):262-74. doi: 10.2174/156652312802083594.
Exosomes are a subtype of membrane vesicle released from the endocytic compartment of live cells. They play an important role in endogenous cell-to-cell communication. Previously shown to be capable of traversing biological barriers and to naturally transport functional nucleic acids between cells, they potentially represent a novel and exciting drug delivery vehicle for the field of gene therapy. Existing delivery vehicles are limited by concerns regarding their safety, toxicity and efficacy. In contrast, exosomes, as a natural cell-derived nanocarrier, are immunologically inert if purified from a compatible cell source and possess an intrinsic ability to cross biological barriers. Already utilised in a number of clinical trials, exosomes appear to be well-tolerated, even following repeat administration. Recent studies have shown that exosomes may be used to encapsulate and protect exogenous oligonucleotides for delivery to target cells. They therefore may be valuable for the delivery of RNA interference and microRNA regulatory molecules in addition to other single-stranded oligonucleotides. Prior to clinical translation, this nanotechnology requires further development by refinement of isolation, purification, loading, delivery and targeting protocols. Thus, exosome-mediated nanodelivery is highly promising and may fill the void left by current delivery methods for systemic gene therapy.
外泌体是从活细胞的内体区室释放的膜囊泡的一种亚型。它们在细胞内的内源性通讯中起着重要作用。先前已证明它们能够穿越生物屏障,并在细胞之间自然地运输功能性核酸,因此它们有可能成为基因治疗领域中一种新颖而令人兴奋的药物传递载体。现有的传递载体受到对其安全性、毒性和功效的担忧的限制。相比之下,外泌体作为一种天然的细胞衍生的纳米载体,如果从相容的细胞来源中纯化出来,具有免疫惰性,并具有内在的穿越生物屏障的能力。外泌体已经在许多临床试验中得到应用,即使在重复给药后,也似乎具有良好的耐受性。最近的研究表明,外泌体可用于封装和保护外源性寡核苷酸,以递送至靶细胞。因此,除了其他单链寡核苷酸外,它们可能对 RNA 干扰和 microRNA 调节分子的递送很有价值。在临床转化之前,这种纳米技术需要通过改进分离、纯化、加载、递送和靶向方案来进一步发展。因此,外泌体介导的纳米递送具有很高的应用前景,可能会填补当前系统基因治疗方法留下的空白。